Betula papyrifera - Unknown
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Internal ID UUID643ff0f083cb2421078478
Scientific name Betula papyrifera
Authority Marshall
First published in Arbust. Amer. : 19 (1785)

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Synonyms Top

Scientific name Authority First published in
Betula alba var. commutata Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 401 (1865)
Betula alba subsp. excelsa (Aiton) Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 405. 1865 (1865)
Betula alba var. papyrifera (Marshall) Spach Ann. Sci. Nat., Bot. , sér. 2, 15: 188 (1841)
Betula davurica var. americana Regel Prodr. 16(2): 175 (1868)
Betula excelsa L. ex B.D.Jacks. Index Linn. Herb. 44 1912), nomen.
Betula grandis Schrad. Index Seminum (GOET, Gottingensis) 1833: 2 (1833)
Betula kenaica W.H.Evans Bot. Gaz. 27: 481 (1899)
Betula latifolia Tausch Flora 21: 751 (1838)
Betula papyrifera var. lyalliana Koehne Handb. Laubholzben. 55 1903
Betula montanensis B.T.Butler Bull. Torrey Bot. Club 36: 438 (1909)
Betula neoalaskana var. kenaica (W.H.Evans) B.Boivin Naturaliste Canad. 94: 230 (1967)
Betula papyracea Aiton Hortus Kew. 3: 337 (1789)
Betula papyrifera var. commutata (Regel) Fernald Rhodora 47: 312 (1945)
Betula papyrifera subsp. commutata (Regel) A.E.Murray Kalmia 12: 18 (1982)
Betula papyrifera var. elobata Sarg. J. Arnold Arbor. 1: 63 (1919)
Betula papyrifera var. kenaica A.Henry in Elwes & A.Henry Trees Great Britain 4: 984 (1909)
Betula papyrifera subsp. kenaica (W.H.Evans) A.E.Murray Kalmia 12: 18 (1982)
Betula papyrifera var. macrostachya Fernald Rhodora 47: 318 (1945)
Betula papyrifera var. pensilis Fernald Rhodora 47: 318 (1945)
Betula papyrifera var. subcordata Sarg. J. Arnold Arbor. 1: 63 (1919)
Betula papyrifera subsp. subcordata (B.T.Butler) A.E.Murray Kalmia 12: 18 (1982)
Betula pirifolia hort. ex K.Koch Dendrologie 2(2): 646 (1873)
Betula subcordata B.T.Butler Bull. Torrey Bot. Club 36: 436 (1909)
Betula alba var. elobata Fernald Rhodora 15: 169 (1913)
Betula alba subsp. papyrifera (Marshall) Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 401 (1865)
Betula kamtschatica var. kenaica (W.H.Evans) C.-A.Jansson Acta Horti Gothob. 25: 137 (1962)
Betula lenta var. papyrifera (Marshall) Castigl. Viagg. Stati Uniti 2: 207 (1790)
Betula papyracea var. grandis (Schrad.) Schelle Handb. Laubholzben. 55. 1903
Betula papyrifera var. andrewsii Daniels Fl. Boulder Colorado : 101 (1911)
Betula papyrifera var. communis Regel Handb. Laubholzben. 1: 115 (1904)
Betula papyrifera f. coriacea Fernald & Wiegand Rhodora 25: 209 (1923)
Betula papyrifera f. elobata (Fernald) B.Boivin Naturaliste Canad. 94: 231 (1967)
Betula papyrifera f. longipes Fernald Rhodora 47: 319 (1945)
Betula papyrifera var. montanensis Sarg. J. Arnold Arbor. 1: 64 (1919)
Betula papyrifera f. nana B.Boivin Naturaliste Canad. 94: 231 (1967)
Betula papyrifera var. recessa Lepage Naturaliste Canad. 89: 115 (1962)
Betula alba subsp. latifolia (Tausch) Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 399. 1865 (1865)
Betula lyalliana (Koehne) Bean Trees & Shrubs Brit. Isles 258. 1914 (1914)
Betula papyracea var. communis (Regel) Schelle Handb. Laubholzben. 55 1903
Betula papyracea var. lyalliana (Koehne) Schelle Handb. Laubholzben. 55 1903

Common names Top

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Language Common/alternative name
English white birch
English silver birch
English paper birch
English canoe birch
Spanish abedul de los cánoes
Spanish abedul papirífero
Spanish abedul papirifero
Spanish american white birch
Spanish canoe birch
Spanish paper birch
Spanish abedul de los canoes
Arabic سندر
atj wikwasatikw
Belarusian Бяроза папяровая
Czech bříza papírovitá
German papierbirke
German kanubirke
German kanu-birke
German amerikanische weißbirke
German amerikanische weiß-birke
German papier-birke
Esperanto papera betulo
Estonian paberikask
Persian توس کاغذی
Finnish paperikoivu
French bouleau à papier
French bouleau á papier
French bouleau blanc
French bouleau à canot
Irish beith gheal
Hebrew שדר הנייר
Hungarian papírnyír
Armenian Կեչի թղթյա
Icelandic næfurbjörk
Japanese アメリカシラカンバ
Lithuanian popieržievis beržas
Latvian papīrbērzs
Norwegian Bokmål papirbjørk
Dutch papierberk
oj wiigwaas
Polish brzoza papierowa
Russian Берёза американская белая
Russian Берёза бумажная
Russian Берёза канойская
Russian Береза бумажная
Slovak breza papierovitá
Serbian Папираста бреза
Swedish pappersbjörk
Turkish kâğıt huşu
tt Ак каен
Chinese 北美白桦
Chinese 北美白樺
Chinese 纸桦
Chinese 凯纳纸皮桦

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Betula papyrifera var. cordifolia (Regel) Regel Bull. Soc. Imp. Naturalistes Moscou 38(2): 401 1865

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Nebraska
      • North Dakota
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • Southeastern U.S.A.
      • Virginia
    • Subarctic America
      • Alaska
      • Northwest Territorie
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000335192
UNII SL7A75J492
Cornell Woody Plants 34
Canadensys 3697
USDA Plants BEPA
UConn 66
Tropicos 3600017
INPN 761871
KEW urn:lsid:ipni.org:names:32197-2
The Plant List kew-21557
Plantarium 46380
Missouri Botanical Garden 242294
PaleoBotany 97694
Open Tree Of Life 267725
Observations.org 137594
NCBI Taxonomy 3507
NBN Atlas NBNSYS0000033441
Nature Serve 2.128519
IUCN Red List 194502
IPNI 32197-2
iNaturalist 49883
GBIF 5332120
Freebase /m/0589lz
WisFlora 2738
FEIS plants/tree/betpap
EPPO BETPA
EOL 1149366
Elurikkus 3101
US Library of Congress sh85097598
USDA GRIN 7122
Wikipedia Betula_papyrifera
CMAUP NPO18986

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Frequent and strong cold‐air pooling drives temperate forest composition Pastore MA, Classen AT, D'Amato AW, English ME, Rand K, Foster JR, Adair EC Ecol Evol 01-Apr-2024
PMCID:PMC10985370
doi:10.1002/ece3.11126
PMID:38571787
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 Strickland LE, Thompson RS, Shafer SL, Bartlein PJ, Pelltier RT, Anderson KH, Schumann RR, McFadden AK Sci Data 12-Jan-2024
PMCID:PMC10786896
doi:10.1038/s41597-023-02616-y
PMID:38216580
Lake Superior's summer cooling of shorelines and adjacent inland forests: Implications for refugia of boreal forests and disjunct arctic–alpine plants Hillman A, Nielsen SE Ecol Evol 28-Dec-2023
PMCID:PMC10753639
doi:10.1002/ece3.10833
PMID:38155816
It takes a village to grow a tree: Most tree species benefit from dissimilar neighbors Di Maurizio V, Searle E, Paquette A Ecol Evol 21-Dec-2023
PMCID:PMC10739099
doi:10.1002/ece3.10804
PMID:38145019
Synthesis, Pharmacological Properties, and Potential Molecular Mechanisms of Antitumor Activity of Betulin and Its Derivatives in Gastrointestinal Cancers Madej M, Gola J, Chrobak E Pharmaceutics 13-Dec-2023
PMCID:PMC10748330
doi:10.3390/pharmaceutics15122768
PMID:38140110
Factors influencing the difference in dissolved ion inputs to the forest floor between deciduous and coniferous stands: comparison under high and low atmospheric deposition conditions Imamura N, Ohte N, Tanaka N Environ Monit Assess 02-Dec-2023
PMCID:PMC10693530
doi:10.1007/s10661-023-12132-6
PMID:38041704
Young temperate tree species show different fine root acclimation capacity to growing season water availability Jaeger FC, Handa IT, Paquette A, Parker WC, Messier C Plant Soil 17-Nov-2023
PMCID:PMC10948563
doi:10.1007/s11104-023-06377-w
PMID:38510944
Scientific opinion on the renewal of the authorisation of SmokEz C‐10 (SF‐005) as a smoke flavouring Primary Product Younes M, Aquilina G, Castle L, Degen G, Engel K, Fowler PJ, Frutos Fernandez MJ, Fürst P, Gundert‐Remy U, Gürtler R, Husøy T, Manco M, Moldeus P, Passamonti S, Shah R, Waalkens‐Berendsen I, Wright M, Benigni R, Boon P, Bolognesi C, Cordelli E, Chipman K, Degen G, Sahlin U, Carfì M, Martino C, Multari S, Palaniappan V, Tard A, Mennes W EFSA J 16-Nov-2023
PMCID:PMC10652705
doi:10.2903/j.efsa.2023.8367
PMID:38027441
Scientific opinion on the renewal of the authorisation of SmokEz Enviro‐23 (SF‐006) as a smoke flavouring Primary Product Younes M, Aquilina G, Castle L, Degen G, Engel K, Fowler PJ, Frutos Fernandez MJ, Fürst P, Gundert‐Remy U, Gürtler R, Husøy T, Manco M, Moldeus P, Passamonti S, Shah R, Waalkens‐Berendsen I, Wright M, Benigni R, Boon P, Bolognesi C, Cordelli E, Chipman K, Sahlin U, Carfì M, Martino C, Multari S, Palaniappan V, Tard A, Mennes W EFSA J 16-Nov-2023
PMCID:PMC10652696
doi:10.2903/j.efsa.2023.8368
PMID:38027452
Thermal adaptation of soil microbial growth traits in response to chronic warming Eng AY, Narayanan A, Alster CJ, DeAngelis KM Appl Environ Microbiol 25-Oct-2023
PMCID:PMC10686086
doi:10.1128/aem.00825-23
PMID:37877729
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Modelling the potential of forest management to mitigate climate change in Eastern Canadian forests Ameray A, Bergeron Y, Cavard X Sci Rep 04-Sep-2023
PMCID:PMC10477314
doi:10.1038/s41598-023-41790-2
PMID:37666929
A trait-based approach to both forestry and timber building can synchronize forest harvest and resilience Osborne P, Aquilué N, Mina M, Moe K, Jemtrud M, Messier C PNAS Nexus 29-Aug-2023
PMCID:PMC10465084
doi:10.1093/pnasnexus/pgad254
PMID:37649582
In This Issue N/A Proc Natl Acad Sci U S A 22-Aug-2023
PMCID:PMC10452279
doi:10.1073/iti3423120

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-dimethoxybenzoate 370912 Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2 272.29 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D 10905866 Click to see CC1=C2CC(C3(C(CCCC3(C2=CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 418.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Lyoniside 14521038 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid 5192 Click to see C(CCCCC(=O)O)CCCC(=O)O 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R,3R,4R,5R)-5,6-dihydroxy-2,3,4-trimethoxyhexanal 163011700 Click to see COC(C=O)C(C(C(CO)O)OC)OC 222.24 unknown https://doi.org/10.1021/JA01504A046
2,3,4-Tri-O-methylhexose 538775 Click to see COC(C=O)C(C(C(CO)O)OC)OC 222.24 unknown https://doi.org/10.1021/JA01504A046
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698321 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 572.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10531102 Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 570.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 6479669 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 464.60 unknown via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 10951647 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)COC(=O)C6=CC=CC=C6 540.60 unknown via CMAUP database
Isovouacapenol A 636673 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 420.50 unknown via CMAUP database
Isovouacapenol B 11812203 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3(C)O)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 438.60 unknown via CMAUP database
Isovouacapenol C 3009285 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 438.60 unknown via CMAUP database
Pulcharrin G 11750983 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)O)O)(C)C)C 438.60 unknown via CMAUP database
Pulcherrimin F 11375664 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)C 510.60 unknown via CMAUP database
Pulcherrin D 54597502 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(CC2OC(=O)C)O)(C)C)C 360.50 unknown via CMAUP database
Pulcherrin E 54597503 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)O)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin F 54597504 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin H 54597566 Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O 422.60 unknown via CMAUP database
Pulcherrin I 54597567 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 422.60 unknown via CMAUP database
Pulcherrin J 54597568 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C=CC5=CC=CC=C5 448.60 unknown via CMAUP database
Pulcherrin K 53388795 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C=O)C 452.50 unknown via CMAUP database
Pulcherrin L 53388797 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O 438.60 unknown via CMAUP database
Pulcherrin M 54597569 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5 452.50 unknown via CMAUP database
Pulcherrin O 53388938 Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1(C(C(CC4)OC(=O)C5=CC=CC=C5)(C)C)O)C)O 540.60 unknown via CMAUP database
Vouacapen-5alpha-ol 73354918 Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 42433495 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 7067459 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
7-Hydroxycadalene 608115 Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O 214.30 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Papyriferic acid 441683 Click to see CC(=O)OC1CC2C3(CCC(C(C3CCC2(C4(C1C(CC4)C5(CCC(O5)C(C)(C)O)C)C)C)(C)C)OC(=O)CC(=O)O)C 604.80 unknown https://doi.org/10.1021/JO00335A054
https://doi.org/10.1002/PCA.2800020209
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bS,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 40884471 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163013840 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 25728252 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1081/SCC-100104070
https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
CID 11954143 11954143 Click to see CC1(CCC23CCC4(C(C2C1OC3)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C)C 442.70 unknown https://doi.org/10.1016/0378-8741(84)90002-3
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97169-3
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10627788 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)OC(=O)C)C 630.70 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11157932 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)OC(=O)C6=CC=CC=C6)C 630.70 unknown via CMAUP database
(8beta,10beta,14alpha)-6beta,7beta-Bis(benzoyloxy)-3beta,5alpha-dihydroxy-12,16-epoxycassa-12,15-dien-19-oic acid 10698605 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)O)C 588.60 unknown via CMAUP database
Pulcherrin N 53388796 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6 572.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
Pulcherrin P 53388939 Click to see CC(=O)OCC1(C(CCC2(C1(C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)OC(=O)C)O)O)C)OC(=O)C5=CC=CC=C5)C 598.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol 162908745 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O 428.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol 4484392 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
2-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol 162908744 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O 428.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Furcatin 442789 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Neocaesalpin E 11450901 Click to see CC1C2CCC3(C(CCCC3(C2CC4(C1=CC(=O)O4)OC)C)(C)C)O 348.50 unknown via CMAUP database
Neocaesalpin F 11386164 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 484.60 unknown via CMAUP database
Neocaesalpin G 11295185 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 510.60 unknown via CMAUP database
Pulcherrin Q 53388940 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(4-hydroxyphenyl)-4-hepten-3-one 53840022 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
2-[1,7-Bis(4-hydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73818247 Click to see C1=CC(=CC=C1CCCCC(CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
aceroside VII 21637601 Click to see C1=CC(=CC=C1CCCCC(CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Platyphyllenone 23786382 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5S)-5-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one 162985559 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC(CCC3=CC=C(C=C3)O)CC(=O)CCC4=CC=C(C=C4)O)CO)O)O)O)(CO)O 608.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
(5S)-5-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one 24179441 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)O 608.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
(5S)-5-[(2R,3R,4S,5S,6R)-6-[[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one 162872386 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)O 608.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
1,7-Bis(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one 14833391 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
5-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one 162985558 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC(CCC3=CC=C(C=C3)O)CC(=O)CCC4=CC=C(C=C4)O)CO)O)O)O)(CO)O 608.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
5-[6-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one 74218419 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)O 608.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Platyphylloside 9826264 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
https://doi.org/10.1016/0305-1978(95)00106-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2R,3R,4S,5R)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]oxy]oxane-3,4,5-triol 97052283 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)O)O 422.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
(2S,3R,4S,5S,6R)-2-[[(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21676369 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Catechin 7-glucoside 14282767 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.018
Quercimeritrin 5282160 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC4=C(C=C3)OCO4)C(=C1)OC 328.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4 326.30 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one 44260091 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O)OC 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-(2,4-Dimethoxybenzylidene)-7-hydroxychroman-4-one 101356812 Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC 312.30 unknown via CMAUP database
(3E)-3-(4-Methoxybenzylidene)-7-methoxychroman-4-one 6507117 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)OC 296.30 unknown via CMAUP database
(3E)-3-[(3,4-dimethoxyphenyl)methylidene]-7-methoxychromen-4-one 5783568 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC(=C(C=C3)OC)OC)CO2 326.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see COC1=CC(=CC(=C1OC)OC)C=C2COC3=C(C2=O)C=CC(=C3)O 342.30 unknown via CMAUP database
3-(4-Hydroxybenzylidene)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one 14079440 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC=C(C=C3)O)CO2 282.29 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 18778791 Click to see C1C(=CC2=CC3=C(C=C2)OCO3)C(=O)C4=C(O1)C=C(C=C4)O 296.27 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one 101489712 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2 310.30 unknown via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-6,7-dimethoxy-2,3-dihydro-4H-1-benzopyran-4-one 44475180 Click to see COC1=C(C=C(C=C1)C=C2COC3=CC(=C(C=C3C2=O)OC)OC)O 342.30 unknown via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 13846662 Click to see COC1=C(C=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)O 298.29 unknown via CMAUP database
Bonducellin 14079439 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
Isobonducellin 10423880 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51533159 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC(=C3)O 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone 10337542 Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O 344.40 unknown via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database

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